Link to this page
Online Mendelian Inheritance in Man
Last uploaded:
March 22, 2026
| Id | http://purl.bioontology.org/ontology/OMIM/614407
http://purl.bioontology.org/ontology/OMIM/614407
|
|---|---|
| Preferred Name | MICROCEPHALY, CEREBELLAR HYPOPLASIA, AND CARDIAC CONDUCTION DEFECT SYNDROME |
| Synonyms |
MCHCCD
ZAKI-GLEESON SYNDROME
|
| Type | http://www.w3.org/2002/07/owl#Class |
All Properties
| altLabel |
MCHCCD
ZAKI-GLEESON SYNDROME
|
|---|---|
| prefLabel | MICROCEPHALY, CEREBELLAR HYPOPLASIA, AND CARDIAC CONDUCTION DEFECT SYNDROME
|
| Scope Statement | One consanguineous Egyptian family with 4 affected individuals has been reported (as of December 2011) [MISCELLANEOUS]
|
| type | |
| Has manifestation |
See more
See less
|
| tui | T047
|
| MIMTYPEMEANING | Mendelian phenotype or locus, molecular basis unknown.
|
| notation | 614407
|
| Semantic type UMLS property | |
| Has inheritance type | |
| cui | C3280692
|
| OMIM Entry Type | 5
|
| OMIM MimType Value | perc
|
| Delete | Subject | Author | Type | Created |
|---|---|---|---|---|
| No notes to display |